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Sulfabromomethazine

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Identification
Molecular formula
C12H13BrN4O2S
CAS number
527-71-1
IUPAC name
4-amino-N-(5-bromo-4,6-dimethyl-pyrimidin-2-yl)benzenesulfonamide
State
State

At room temperature, Sulfabromomethazine is typically in a solid state.

Melting point (Celsius)
183.00
Melting point (Kelvin)
456.15
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
372.23g/mol
Molar mass
372.2250g/mol
Density
1.1900g/cm3
Appearence

Sulfabromomethazine typically appears as a white or off-white crystalline powder. It is often odorless and has a slightly bitter taste.

Comment on solubility

Solubility of 4-amino-N-(5-bromo-4,6-dimethyl-pyrimidin-2-yl)benzenesulfonamide

The solubility of 4-amino-N-(5-bromo-4,6-dimethyl-pyrimidin-2-yl)benzenesulfonamide can be influenced by several factors, which are crucial for understanding its behavior in both aqueous and organic solvents. Here are some significant points to consider:

  • Polarity: The presence of the sulfonamide group tends to enhance its polarity, potentially leading to improved solubility in polar solvents such as water.
  • Temperature Dependency: Like many compounds, solubility can increase with temperature, so evaluating solubility at various temperatures is vital.
  • pH Influence: The ionization of the amino and sulfonamide groups is pH-dependent, which can significantly affect solubility. For instance, at acidic pH, protonation may occur, enhancing its solubility.
  • Interactions with Solvents: Strong hydrogen bonding with the solvent can promote solubility. Consideration of potential interactions with other polar molecules is crucial.

In short, the solubility of this compound is a complex interplay of its molecular structure, solvent characteristics, and environmental conditions. Comprehensive solubility testing under varied conditions will provide a clearer picture of its solubility profile.

Interesting facts

Interesting Facts about 4-amino-N-(5-bromo-4,6-dimethyl-pyrimidin-2-yl)benzenesulfonamide

This compound, known as an important *sulfonamide derivative*, has garnered attention in both medicinal chemistry and agricultural applications. Here are some intriguing aspects:

  • Pharmaceutical Relevance: Sulfonamides were among the first antibiotics discovered, leading to significant advancements in the treatment of bacterial infections. This specific sulfonamide may exhibit potential properties that contribute to drug design.
  • Structure-Activity Relationship (SAR): The presence of the 5-bromo and 4,6-dimethyl groups in the pyrimidine ring enhances the compound's biological activity and stability. Such modifications are crucial for optimizing the efficacy of sulfonamide compounds.
  • Inhibition of Enzymes: Similar to other sulfonamides, this compound may function by inhibiting bacterial *dihydropteroate synthase*, an essential enzyme in folate biosynthesis. This process disrupts the growth of bacteria and can be leveraged in developing novel antimicrobial agents.
  • Potential Use in Agriculture: Beyond medicinal applications, sulfonamides can be utilized as herbicides or fungicides, capitalizing on their ability to inhibit specific biochemical pathways in plants. This opens doors for developing safer agricultural chemicals.
  • Research Opportunities: Scientists are continuously exploring the anti-inflammatory properties and effects against various diseases, such as cancer. The intricate design of this compound invites extensive research to uncover novel therapeutic potentials.

As it stands, 4-amino-N-(5-bromo-4,6-dimethyl-pyrimidin-2-yl)benzenesulfonamide represents a fascinating intersection of synthetic chemistry and drug development, pushing the boundaries of what sulfonamide derivatives can achieve.

Synonyms
Sulfabrom
SULFABROMOMETHAZINE
116-45-0
5-Bromosulfamethazine
Bromosulfamethazine
4-amino-N-(5-bromo-4,6-dimethylpyrimidin-2-yl)benzenesulfonamide
UNII-PQK2N461KJ
NSC 5874
NSC-5874
PQK2N461KJ
DTXSID5046857
NSC5874
S. N. 3517
EINECS 204-142-6
N 3517;Sulfabromomethazine
SULFABROMOMETHAZINE [MI]
DTXCID3026857
CHEBI:145405
Benzenesulfonamide, 4-amino-N-(5-bromo-4,6-dimethyl-2-pyrimidinyl)-
N1-(5-bromo-4,6-dimethyl-2-pyrimidinyl)sulfanilamide
NCGC00181118-01
4-Amino-N-(5-bromo-4,6-dimethyl-2-pyrimidinyl)benzenesulfonamide
Sulfabromomethazine sodium
Sulfanilamide, N1-(5-bromo-4,6-dimethyl-2-pyrimidinyl)-
4-amino-N-(5-bromo-4,6-dimethylpyrimidin-2-yl)benzene-1-sulfonamide
N(SUP 1)-(5-BROMO-4,6-DIMETHYL-2-PYRIMIDINYL)SULFANILAMIDE
4-Amino-N-(5-bromo-4,6-dimethyl-2-pyrimidinyl)benzenesulphonamide
SCHEMBL93972
CHEMBL2111078
KWXCNODTHBHSIQ-UHFFFAOYSA-N
EX-A7616
Tox21_112729
HY-U00131
AKOS030586382
CS-7168
DB11547
SB58329
CAS-116-45-0
DA-58162
MS-25598
NS00011880
5-Bromo-4,6-dimethyl-2-sulfanilamidopyrimidine
G13249
Q27286710
Sulfanilamide, N1-(5-bromo-4,6-dimethyl-2-pyrimidinyl)-(8CI)
4-AMINO-N-(5-BROMO-4,6-DIMETHYL-PYRIMIDIN-2-YL)BENZENESULFONAMIDE
Benzenesulfonamide, 4-amino-N-(5-bromo-4,6-dimethyl-2-pyrimidinyl)-(9CI)
204-142-6